Glucose Control in Pre-Diabetic Renal Transplant Patients (GCPD)
Primary Purpose
Impaired Glucose Tolerance, Kidney Transplantation
Status
Completed
Phase
Phase 2
Locations
Austria
Study Type
Interventional
Intervention
Vildagliptin
Pioglitazone
Life-Style Modification
Sponsored by
About this trial
This is an interventional treatment trial for Impaired Glucose Tolerance focused on measuring after
Eligibility Criteria
Inclusion Criteria:
- Time since renal transplantation > 6 months
- Stable graft function
- Routine OGTT has been performed, and pre-diabetes has been diagnosed by pathological OGTT (2h, 75 g glucose, glucose level between 140 and 200 mg/dl)
- Informed consent of the patient
Exclusion Criteria:
- Patients with type 1 or type 2 diabetes
- Patients with NODAT (2h glucose level at OGTT >200 mg/dl)
- allergy against vildagliptin or pioglitazone
- pregnancy
- GFR<15ml/min/1.73 with need for dialysis
- hepatic impairment
Sites / Locations
- Allgemeines Krankenhaus der Stadt Wien, Universitätskliniken
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Experimental
Placebo Comparator
Arm Label
Vildagliptin
Pioglitazone
Placebo
Arm Description
16 patients randomized into this arm will receive vildagliptin (Galvus) 50mg orally once daily
16 patients randomized into this arm will receive pioglitazone (Actos) 30mg orally once daily
16 patients randomized into this arm will receive placebo medication orally once daily
Outcomes
Primary Outcome Measures
Oral glucose tolerance test (OGTT)
Glucose tolerance and insulin resistance three months after study start will be measured by means of a frequent sampling OGTT (75g glucose, determination of glucose, insulin and C-peptide) over 120 mins.
Secondary Outcome Measures
glycated hemoglobin
HbA1c will be measured after three months and compared between the study arms
Renal function
Renal function will be assessed by measuring serum creatinin and glomerular filtration rate (GFR)at the beginning of the study and after three months of treatment
Liver function
Liver enzymes (ALAT, ASAT, Gamm-GT) will be measured at the start of the study and after three months treatment
Lipid profiles
Lipid profiles will be analyzed at the beginning and end of the study including Cholesterol, HDL, LDL and triglycerides.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01346254
Brief Title
Glucose Control in Pre-Diabetic Renal Transplant Patients
Acronym
GCPD
Official Title
Glucose Control in Pre-Diabetic Renal Transplant Patients: Efficacy and Safety of Vildagliptin and Pioglitazone
Study Type
Interventional
2. Study Status
Record Verification Date
December 2011
Overall Recruitment Status
Completed
Study Start Date
December 2009 (undefined)
Primary Completion Date
November 2011 (Actual)
Study Completion Date
November 2011 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Marcus Saemann
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Development of New-Onset Diabetes after Transplantation (NODAT) is common and serious complication after kidney transplantation. Patients who develop NODAT are at increased risk for loss of the transplanted organ and for diseases of the cardiovascular system.
It is believed that in many patients the development of overt NODAT is preceded by a phase of impaired glucose tolerance that is called pre-diabetes.
This study aims at improving glucose metabolism in patients after kidney transplantation who are in a pre-diabetic metabolic state. Patients who exhibit impaired glucose tolerance (IGT) after kidney transplantation are randomized to either receive vildagliptin (Galvus), pioglitazone(Actos) or placebo for three months.
The investigators hypothesize that treatment with vildagliptin or pioglitazone leads to improved glycemic control compared to placebo.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Impaired Glucose Tolerance, Kidney Transplantation
Keywords
after
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
51 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Vildagliptin
Arm Type
Experimental
Arm Description
16 patients randomized into this arm will receive vildagliptin (Galvus) 50mg orally once daily
Arm Title
Pioglitazone
Arm Type
Experimental
Arm Description
16 patients randomized into this arm will receive pioglitazone (Actos) 30mg orally once daily
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
16 patients randomized into this arm will receive placebo medication orally once daily
Intervention Type
Drug
Intervention Name(s)
Vildagliptin
Other Intervention Name(s)
Galvus
Intervention Description
50mg tablets once daily 20 min before breakfast for 3 months
Intervention Type
Drug
Intervention Name(s)
Pioglitazone
Other Intervention Name(s)
Actos
Intervention Description
30mg tablets once daily 20 min before breakfast for 3 months
Intervention Type
Behavioral
Intervention Name(s)
Life-Style Modification
Intervention Description
All study participants were counselled regarding life-style modification including regular exercise, weight loss and diet.
Primary Outcome Measure Information:
Title
Oral glucose tolerance test (OGTT)
Description
Glucose tolerance and insulin resistance three months after study start will be measured by means of a frequent sampling OGTT (75g glucose, determination of glucose, insulin and C-peptide) over 120 mins.
Time Frame
three months
Secondary Outcome Measure Information:
Title
glycated hemoglobin
Description
HbA1c will be measured after three months and compared between the study arms
Time Frame
3 months
Title
Renal function
Description
Renal function will be assessed by measuring serum creatinin and glomerular filtration rate (GFR)at the beginning of the study and after three months of treatment
Time Frame
3 months
Title
Liver function
Description
Liver enzymes (ALAT, ASAT, Gamm-GT) will be measured at the start of the study and after three months treatment
Time Frame
3 months
Title
Lipid profiles
Description
Lipid profiles will be analyzed at the beginning and end of the study including Cholesterol, HDL, LDL and triglycerides.
Time Frame
3 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
81 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Time since renal transplantation > 6 months
Stable graft function
Routine OGTT has been performed, and pre-diabetes has been diagnosed by pathological OGTT (2h, 75 g glucose, glucose level between 140 and 200 mg/dl)
Informed consent of the patient
Exclusion Criteria:
Patients with type 1 or type 2 diabetes
Patients with NODAT (2h glucose level at OGTT >200 mg/dl)
allergy against vildagliptin or pioglitazone
pregnancy
GFR<15ml/min/1.73 with need for dialysis
hepatic impairment
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marcus Säemann, MD
Organizational Affiliation
Medical University of Vienna, Department of Internal Medicine III, Division of Nephrology and Dialysis
Official's Role
Principal Investigator
Facility Information:
Facility Name
Allgemeines Krankenhaus der Stadt Wien, Universitätskliniken
City
Wien
ZIP/Postal Code
1090
Country
Austria
12. IPD Sharing Statement
Citations:
PubMed Identifier
32803882
Citation
Lo C, Toyama T, Oshima M, Jun M, Chin KL, Hawley CM, Zoungas S. Glucose-lowering agents for treating pre-existing and new-onset diabetes in kidney transplant recipients. Cochrane Database Syst Rev. 2020 Jul 30;8(8):CD009966. doi: 10.1002/14651858.CD009966.pub3.
Results Reference
derived
Learn more about this trial
Glucose Control in Pre-Diabetic Renal Transplant Patients
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